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(R)-(+)-O-methyl tert-butylphenylphosphinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69460-42-0

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69460-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69460-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,6 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69460-42:
(7*6)+(6*9)+(5*4)+(4*6)+(3*0)+(2*4)+(1*2)=150
150 % 10 = 0
So 69460-42-0 is a valid CAS Registry Number.

69460-42-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-(+)-O-methyl tert-butylphenylphosphinate

1.2 Other means of identification

Product number -
Other names (R)-methyl t-butylphenylphosphinate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69460-42-0 SDS

69460-42-0Downstream Products

69460-42-0Relevant academic research and scientific papers

Reactions of (RP)- and (SP)-tert-butylphenylphosphinobromidates and tert-butylphenylthionophosphinochloridates with heteroatom nucleophiles; preparation of P-chiral binol phosphinates and related compounds

Au-Yeung, Tin-Lok,Chan, Ka-Yee,Chan, Wai-Kuen,Haynes, Richard K.,Williams, Ian D.,Yeung, Lam Lung

, p. 453 - 456 (2007/10/03)

Reaction of (RP)- and (SP)-tert-butylphenylphosphinobromidates and tert-butylphenylthionophosphinochloridates with metallated phenol and BINOL alkoxides, thioalkoxides, amides and enolates leading with clean inversion at phosphorus t

New procedures for the resolution of chiral tert-butylphenylphosphine oxide and some of its reactions

Drabowicz, Joezef,Lyzwa, Piotr,Omelanczuk, Jan,Pietrusiewicz, K. Michal,Mikolajczyk, Marian

, p. 2757 - 2763 (2007/10/03)

Racemic t-butylphenylphosphine oxide was resolved via formation of diastereoisomeric complexes with (+)-(R)-1,1'-binaphthalene-2,2'-diol and (+)-(S)-mandelic acid. With the latter complexing agent, separation of the essentially enantiopure (-)-(S)-enantio

Reaction of Thiolo and Selenolo Esters of Phosphorus Acids with Halogens. Part 2. Interaction of S-Methyl t-Butyl(phenyl)- and Di-t-butyl-phosphinothiolates with Elemental Bromine and Iodine

Krawiecka, Bozena,Wojna-Tadeusiak, Elzbieta

, p. 301 - 309 (2007/10/02)

The reaction of S-methyl t-butyl(phenyl)- and di-t-butyl-phosphinothiolates with bromine and iodine involves the transient formation of the same type of halosulphonium salts, ButRP(O)S+(X)MeX- and phosphonium salts, Busup

Reaction of Thiolo and Seleno Esters of Phosphorus Acids with Halogens. 1. Stereochemical and 31P NMR Studies of Reaction of S-Methyl tert-Butylphenylphosphinothiolate with Elemental Chlorine and Sulfuryl Chloride

Krawiecka, B.,Michalski, J.,Wojna-Tadeusiak, E.

, p. 4201 - 4208 (2007/10/02)

Reaction of S-methyl tert-butylphenylphosphinothiolate (4) with elemental chlorine and sulfuryl chloride involves chlorolysis of the P-S bond and formation of the tert-butylphenylphosphinochloridate 5.It is demonstrated here that the stereoselectivity of

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